质量水平
检测方案
≥95%
形式
liquid
环保替代产品特性
Safer Solvents and Auxiliaries
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
折射率
n/D 1.50625
密度
1.32 g/mL
环保替代产品分类
, Aligned
储存温度
2-8°C
SMILES字符串
[H][C@]1(C=CC2=O)CO[C@]2([H])O1
InChI
1S/C6H6O3/c7-5-2-1-4-3-8-6(5)9-4/h1-2,4,6H,3H2/t4-,6+/m0/s1
InChI key
HITOXZPZGPXYHY-UJURSFKZSA-N
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相关类别
一般描述
We are committed to bringing you greener alternative products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is biorenewable and thus aligns with ″Safer Solvents and Auxiliaries″ and ″Use of Renewable Feedstocks″. Click here for more information.
Levoglucosenone undergoes Michael-addition reaction with diethyl malonate, ethyl cyanoacetate, 2-nitropropane and 2-methylcyclohexanone in the presence of various catalysts to afford 4-substituted levoglucosenone derivatives having the D-erythro configuration.
Levoglucosenone undergoes Michael-addition reaction with diethyl malonate, ethyl cyanoacetate, 2-nitropropane and 2-methylcyclohexanone in the presence of various catalysts to afford 4-substituted levoglucosenone derivatives having the D-erythro configuration.
应用
Levoglucosenone may be used in the synthesis of the following:
- Various deoxy, keto and branched-chain sugars
- 4-thio and 4-substituted sugar derivatives
- Natural stereoisomer of serricornin
警示用语:
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Recent Applications of Levoglucosenone as Chiral Synthon.
Current Organic Synthesis, 9(4), 439-459 (2012)
Natural product reports, 37(3), 380-424 (2019-10-19)
Covering: up to mid-2019 This review highlights the utilization of biomass-derived building blocks in the total synthesis of natural products. An overview over several renewable feedstock classes, namely wood/lignin, cellulose, chitin and chitosan, fats and oils, as well as terpenes
Levoglucosenone and Its New Applications: Valorization of Cellulose Residues.
European Journal of Organic Chemistry, 590-604 (2018)
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